DFNB31 homepage - CCHMC Molecular Genetics Laboratory Mutation Database - Leiden Open Variation Database

CCHMC Molecular Genetics Laboratory Mutation Database

deafness, autosomal recessive 31 (DFNB31)

LOVD v.2.0 Build 36 [ Current LOVD status ]
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Curator: Ammar Husami

DFNB31 homepage

General information
Gene name	deafness, autosomal recessive 31
Gene symbol	DFNB31
Chromosome Location	9q32-q34
Database location	https://research.cchmc.org/LOVD2/
Curator	Ammar Husami
PubMed references	View all (unique) PubMed references in the DFNB31 database
Date of creation	November 18, 2008
Last update	April 23, 2010
Version	DFNB31 100423
Add sequence variant	Submit a sequence variant
First time submitters	Register here
Reference sequence file	Genomic reference sequence for describing sequence variants
Genomic refseq ID	NC_000009.10
Transcript refseq ID	NM_015404.2
Exon/intron information	Exon/intron information table
Total number of unique DNA variants reported	20
Total number of individuals with variant(s)	2
Total number of variants reported	20
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Graphical displays and utilities
Summary tables	Summary of all sequence variants in the DFNB31 database, sorted by type of variant (with graphical displays and statistics)
Reading-frame checker	The Reading-frame checker generates a prediction of the effect of whole-exon changes
UCSC Genome Browser	Show variants in the UCSC Genome Browser (compact view)
Ensembl Genome Browser	Show variants in the Ensembl Genome Browser (compact view)
NCBI Sequence Viewer	Show distribution histogram of variants in the NCBI Sequence Viewer

Sequence variant tables
Unique sequence variants	Listing of all unique sequence variants in the DFNB31 database, without patient data
Complete sequence variant listing	Listing of all sequence variants in the DFNB31 database
Variants with no known pathogenicity	Listing of all DFNB31 variants reported to have no noticeable phenotypic effect (note: excluding variants of unknown effect)
Download table	Download the full sequence variant table of the DFNB31 database in tab-delimited text format.

Search the database
By type of variant	View all sequence variants of a certain type
Simple search	Query the database by selecting the most important variables (exon number, type of variant, disease phenotype)
Advanced search	Query the database by selecting a combination of variables
Based on patient origin	View all variants based on your patient origin search terms

Links to other resources
Entrez Gene	25861
OMIM - Gene	607928
HGMD	DFNB31
GeneTests	DFNB31

For research use. Husamia et al. 2006-2010